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Informed consent prior to coronary angiography in a real world scenario: what do patients remember?
Aslihan Eran1, Erland Erdmann, Fikret Er
1Department of Internal Medicine III, University of Cologne, Cologne, Germany.
Insights
Patients undergoing cardiac angiography (CA) often have poor recall of information provided during informed consent. Even specialized physician training did not significantly improve patient knowledge of potential complications.
Area of Science:
- Cardiology
- Medical Ethics
- Patient Education
Background:
- Informed consent is a legal requirement for cardiac angiography (CA).
- Patient recall of detailed information pre-procedure is not well understood.
- Optimal information delivery scenarios are compared to standard care.
Purpose of the Study:
- To assess patient recall of information provided during informed consent for CA.
- To compare information retention between patients receiving standard care versus information from specially trained physicians.
Main Methods:
- Prospective cohort study of 200 patients (150 in-patients, 50 out-patients) before elective CA.
- In-patients received information from trained physicians; out-patients received standard information.
- Patient knowledge assessed via questionnaire one hour before CA.
Main Results:
- Despite feeling informed (95%), patients recalled less than half of potential complications.
- Less serious complications were remembered more often than life-threatening ones.
- No significant knowledge difference was found between in-patients and out-patients.
Conclusions:
- Patient knowledge regarding cardiac angiography is often vague at the time of informed consent.
- Structured information delivery by trained physicians did not enhance patient knowledge recall.
- Further research is needed to improve patient understanding and informed consent effectiveness.
Background:
Patients' informed consent is legally essential before elective invasive cardiac angiography (CA) and successive intervention can be done. It is unknown to what extent patients can remember previous detailed information given by a specially trained doctor in an optimal scenario as compared to standard care.
Methodology/Principal Findings:
In this prospective cohort study 150 consecutive in-patients and 50 out-patients were included before elective CA was initiated. The informed consent was provided and documented in in-patients by trained and instructed physicians the day before CA. In contrast, out-patients received standard information by different not trained physicians, who did not know about this investigation. All patients had to sign a form stating that enough information had been given and all questions had been answered sufficiently. One hour before CA an assessment of the patients' knowledge about CA was performed using a standard point-by-point questionnaire by another independent physician. The supplied information was composed of 12 potential complications, 3 general, 4 periprocedural and 4 procedural aspects. 95% of the patients felt that they had been well and sufficiently informed. Less than half of the potential complications could be remembered by the patients and more patients could remember less serious than life-threatening complications (27.9±8.8% vs. 47.1±11.0%; p<0.001). Even obvious complications like local bleeding could not be remembered by 35% of in-patients and 36% of out-patients (p = 0.87). Surprisingly, there were only a few knowledge differences between in- and out-patients.
Conclusions:
The knowledge about CA of patients is vague when they give their informed consent. Even structured information given by a specially trained physician did not increase this knowledge.
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